Sulfide-linked 3,4,5-trimethoxyphenyl-thiosemicarbazide/triazole hybrids: Synthesis, antioxidant, antiglycation, DNA cleavage and DNA molecular docking studies

Synthesis and Antioxidant Activity of New Catechol Thioethers with the Methylene Linker

(2022) Ivan V. Smolyaninov et al.   MOLECULES

Development, Molecular Docking, and In Silico ADME Evaluation of Selective ALR2 Inhibitors for the Treatment of Diabetic Complications via Suppression of the Polyol Pathway

(2022) Aqeel Imran et al.   ACS Omega

Design and antiproliferative and antioxidant activities of furan-based thiosemicarbazides and 1,2,4-triazoles: their structure-activity relationship and SwissADME predictions

(2021) Yusuf Sicak   MEDICINAL CHEMISTRY RESEARCH

Structure-antioxidant activity relationship of methoxy, phenolic hydroxyl, and carboxylic acid groups of phenolic acids

(2020) Jinxiang Chen et al.   Scientific Reports

Antioxidant and tyrosinase docking studies of heterocyclic sulfide derivatives containing a thymol moiety

(2020) Mia H. Havasi et al.   INORGANICA CHIMICA ACTA

Oxidative stress mitigation by antioxidants - An overview on their chemistry and influences on health status

(2020) Aurelia Magdalena Pisoschi et al.   EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY

A review on development of bio-active thiosemicarbazide derivatives: Recent advances

(2020) Prachi T. Acharya et al.   JOURNAL OF MOLECULAR STRUCTURE

Heterocyclic β-keto sulfide derivatives of carvacrol: Synthesis and copper (II) ion reducing capacity

(2019) Alexander H. Cocolas et al.   BIOORGANIC & MEDICINAL CHEMISTRY LETTERS

Evaluation of Polyphenol Anthocyanin-Enriched Extracts of Blackberry, Black Raspberry, Blueberry, Cranberry, Red Raspberry, and Strawberry for Free Radical Scavenging, Reactive Carbonyl Species Trapping, Anti-Glycation, Anti-β-Amyloid Aggregation, and Microglial Neuroprotective Effects

(2018) Hang Ma et al.   INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES

Synthesis, in Vitro Biological Evaluation, and Oxidative Transformation of New Flavonol Derivatives: The Possible Role of the Phenyl-N,N-Dimethylamino Group

(2018) Peter Szabados-Furjesi et al.   MOLECULES

Antioxidant and Oxidative Stress: A Mutual Interplay in Age-Related Diseases

(2018) Bee Ling Tan et al.   Frontiers in Pharmacology

Polyphenols with antiglycation activity and mechanisms of action: A review of recent findings

(2017) Wan-Ju Yeh et al.   JOURNAL OF FOOD AND DRUG ANALYSIS

Synthesis of novel coumarin nucleus-based DPA drug-like molecular entity: In vitro DNA/Cu(II) binding, DNA cleavage and pro-oxidant mechanism for anticancer action

(2017) Saman Khan et al.   PLoS One

Development of Multifunctional Pyrimidinylthiourea Derivatives as Potential Anti-Alzheimer Agents

(2016) Xiaokang Li et al.   JOURNAL OF MEDICINAL CHEMISTRY

Conjugated Oligo-Aromatic Compounds Bearing a 3,4,5-Trimethoxy Moiety: Investigation of Their Antioxidant Activity Correlated with a DFT Study

(2016) Huda. Kareem et al.   MOLECULES

Correlation of antioxidant activities with theoretical studies for new hydrazone compounds bearing a 3,4,5-trimethoxy benzyl moiety

(2015) Huda S. Kareem et al.   EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY

New Thiosemicarbazides and 1,2,4-Triazolethiones Derived from 2-(Ethylsulfanyl) Benzohydrazide as Potent Antioxidants

(2014) Nafal Nazarbahjat et al.   MOLECULES

Redox cycling of Cu(II) by 6-mercaptopurine leads to ROS generation and DNA breakage: possible mechanism of anticancer activity

(2014) Sayeed Ur Rehman et al.   TUMOR BIOLOGY

Inhibition of protein glycation by urea and thiourea derivatives of glycine/proline conjugated benzisoxazole analogue – Synthesis and structure–activity studies

(2012) C.S. Shantharam et al.   EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY

A comprehensive review of CUPRAC methodology

(2011) Mustafa Özyürek et al.   Analytical Methods

Copper-mediated nuclease activity of jadomycin B

(2011) Susan M.A. Monro et al.   BIOORGANIC & MEDICINAL CHEMISTRY

Synthesis of bis-Schiff bases of isatins and their antiglycation activity

(2009) Khalid Mohammed Khan et al.   BIOORGANIC & MEDICINAL CHEMISTRY